Stryker Howmedica Osteonics Corp. Gamma System, Cross Screw, Self-Tapping (Cleared under Grosse and Kempf Locking Nail System) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gamma System, Cross Screw, Self-Tapping (Cleared under Grosse and Kempf Locking Nail System)
Brand
Stryker Howmedica Osteonics Corp.
Lot Codes / Batch Numbers
Catalog No 3370-5-035 to 3370-5-090
Products Sold
Catalog No 3370-5-035 to 3370-5-090
Stryker Howmedica Osteonics Corp. is recalling Gamma System, Cross Screw, Self-Tapping (Cleared under Grosse and Kempf Locking Nail System) due to Stryker Orthopaedics was informed by the manufacturer, that in some instances, the sterile blister package of the referenced G/K, T2 condyle and some . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stryker Orthopaedics was informed by the manufacturer, that in some instances, the sterile blister package of the referenced G/K, T2 condyle and some S2 screw products may become damaged during shipping and handling which may result in a potential breach of the sterile barrier.
Recommended Action
Per FDA guidance
The product recall will extend to all branches.agencies and hospitals that have received the product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026